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引用本文:谢明华,蔡鑫君,封玲,葛敏,高建青.利多卡因微乳凝胶剂的制备及初步药效学研究[J].中国现代应用药学,2015,32(4):442-446.
XIE Minghua,CAI Xinjun,FENG Ling,GE min,GAO Jianqing.Preparation and Preliminary Pharmacodynamics of Llidocaine Gel-microemulsion[J].Chin J Mod Appl Pharm(中国现代应用药学),2015,32(4):442-446.
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利多卡因微乳凝胶剂的制备及初步药效学研究
谢明华1,2, 蔡鑫君3, 封玲4, 葛敏2, 高建青1
1.浙江大学,杭州 310058;2.杭州市余杭区第一人民医院,杭州 311100;3.浙江省中西医结合医院,杭州 310003;4.浙江中医药大学,杭州 310000
摘要:
目的 制备利多卡因微乳凝胶剂,并对其药效学及皮肤刺激性进行初步研究。方法 以油酸乙酯为油相,聚山梨酯-80为表面活性剂,无水乙醇为助表面活性剂,用水滴定的方法制备利多卡因微乳。以卡波姆940为凝胶骨架,采用直接溶胀法制备利多卡因微乳凝胶。采用Zetasizer Nano-ZS90马尔文激光粒度仪测定微乳的粒径。采用日立H-7650透射电子显微镜观察微乳的形态。采用热板法观察该药对小鼠的镇痛作用。采用连续给药的方法,考察该药对家兔正常皮肤与破损皮肤的刺激性。结果 利多卡因微乳凝胶外观为白色透明凝胶态,微乳呈圆球形,微乳粒径<100 nm。利多卡因微乳凝胶剂能延长热板致痛的潜伏期,对家兔皮肤无刺激性。结论 利多卡因微乳凝胶剂具有较好的局麻镇痛作用和安全性。
关键词:  利多卡因微乳凝胶剂  镇痛  药效学  皮肤刺激性
DOI:
分类号:
基金项目:杭州市余杭区科技计划项目(201209);浙江省药学会医院药学专项科研基金项目(2012ZYY17)
Preparation and Preliminary Pharmacodynamics of Llidocaine Gel-microemulsion
XIE Minghua1,2, CAI Xinjun3, FENG Ling4, GE min2, GAO Jianqing1
1.Zhejiang University, Hangzhou 310058, China;2.The First People’s Hospital of Yuhang District, Hangzhou 311100, China;3.Integtated Chinese and Western Medicine Hospital of Zhejiang Province, Hangzhou 310003, China;4.Zhejiang University of Traditional Chinese Medicine, Hangzhou 310000, China
Abstract:
OBJECTIVE To prepare llidocaine gel-microemulsion, and study the pharmacodynamic effects of llidocaine gel-microemulsion. METHODS To use ethylis oleate as oil phase, Polysorbate 80 as surfactant, ethanol as cosurfactant, we prepared lidocaine microemulsion by water titration method. With Carbopol 940 as a substrate, we prepared microemulsion-based gel of lidocaine by direct swelling method. To measure particle size of lidocaine microemulsion with Zetasizer Nano-ZS90. With transmission electron microscope, to observe the lidocaine microemulsion morphologic. With hot plate, the antinociception effects of the drug in mice was observed. To study the Skin irritation by the method of continuous administration of the drug. RESULTS The appearance of llidocaine gel-microemulsion was transparent white gel, the shape of microemulsion was sphere, Particle size of microemulsion was less than 100 nm. Llidocaine gel-microemulsion had the significant effect of the analgesic, it caused no irritability to rabbit skin. CONCLUSION Llidocaine gel-microemulsion has good analgesic effects and safety.
Key words:  llidocaine gel-microemulsion  analgesic  pharmacodynamic  skin irritation
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